Chromosome abnormalities in a referred population for suspected chromosomal aberrations: a report of 4117 cases

J Korean Med Sci. 1999 Aug;14(4):373-6. doi: 10.3346/jkms.1999.14.4.373.

Abstract

A cytogenetic study was performed on 4,117 Korean patients referred for suspected chromosomal abnormalities. Chromosome aberrations were identified in 17.5% of the referred cases. The most common autosomal abnormality was Down syndrome and Turner syndrome in abnormalities of sex chromosome. The proportions of different karyotypes in Down syndrome (trisomy 21 92.5%, translocation 5.1%, mosaic 2.4%) were similar to those reported in other countries. However, it was different in Turner syndrome (45, X 28.1%, mosaic 50.8%, 46, X, del (Xq) 4.4%, 46, X, i (Xq) 16.7%), in which proportions of mosaics and isochromosome, 46, X, i(Xq), were higher than those reported in other countries. In structural chromosome aberrations of autosome, translocation was the most common (43.6%), and duplication (21.3%), deletion (14.4%), marker chromosome (7.9%) and ring chromosome (4.0%) followed in order of frequency. Rates of several normal variant karyotypes were also described. Inversion of chromosome 9 was observed in 1.7% of total referred cases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Chromosome Inversion
  • Chromosomes, Human, Pair 6
  • Down Syndrome / epidemiology*
  • Down Syndrome / genetics*
  • Family Health
  • Female
  • Gene Deletion
  • Humans
  • Infant, Newborn
  • Karyotyping
  • Klinefelter Syndrome / epidemiology
  • Klinefelter Syndrome / genetics
  • Korea / epidemiology
  • Male
  • Mosaicism
  • Prevalence
  • Translocation, Genetic
  • Turner Syndrome / epidemiology*
  • Turner Syndrome / genetics*
  • X Chromosome
  • Y Chromosome